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FDA 510(k)

META - HEALTH MODEL MTG III

K-Number: K861771 · 1986-06-30

ApplicantMeta Health, Inc.
Decision Date1986-06-30
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

META - HEALTH MODEL MTG III is the device name listed in this FDA 510(k) record. The listed applicant is Meta Health, Inc.. It received FDA 510(k) clearance on 1986-06-30 under 510(k) number K861771. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the META - HEALTH MODEL MTG III?

META - HEALTH MODEL MTG III is a medical device that received FDA 510(k) clearance on 1986-06-30. The listed applicant is Meta Health, Inc.. The 510(k) number is K861771.

When did META - HEALTH MODEL MTG III receive FDA 510(k) clearance?

META - HEALTH MODEL MTG III received FDA 510(k) clearance on 1986-06-30, under 510(k) number K861771.

Who is the listed applicant for META - HEALTH MODEL MTG III?

The FDA 510(k) record lists Meta Health, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for META - HEALTH MODEL MTG III?

The FDA product code for META - HEALTH MODEL MTG III is FLL.

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Related Devices (Code: FLL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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